Allele Registry

Canonical Allele Identifier: PA645485982

Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 373003

ClinVar RCV Id: RCV000414646 RCV000418758 RCV000419887 RCV000420910 RCV000420139 RCV000424220 RCV000422093 RCV000427364 RCV000428418 RCV000436881 RCV000429704 RCV000438233 RCV000431603 RCV000434043 RCV000437158 RCV000444600 RCV000429512 RCV000439006 RCV000439308 RCV001813470

ClinVar Variation Id: 375871

ClinVar RCV Id: RCV000426637 RCV000436751 RCV000443672

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gln61His	CA16042285 NM_002524.5:c.183A>T CA16602358 NM_002524.5:c.183A>C